FDA 510(k) Applications Submitted by Double Medical Technology Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K220921 03/30/2022 Metal Bone Screw Double Medical Technology Inc.
K221088 04/13/2022 Anatomic Bone Plate Double Medical Technology Inc.
K221090 04/13/2022 Metal Cannulated Screw Double Medical Technology Inc.
K221150 04/20/2022 Advanced Bone Plate Double Medical Technology Inc.
K221221 04/27/2022 Advanced Intramedullary Nail System Double Medical Technology Inc.
K172830 09/18/2017 Double Medical Femoral Nail System Double Medical Technology Inc.
K223753 12/14/2022 Cervical Plate System Double Medical Technology Inc.


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